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Journal Abstract Search

467 related items for PubMed ID: 8281273

  • 1. Hunter-McAlpine syndrome: report of a third family.
    Adès LC, Morris LL, Simpson DA, Haan EA.
    Clin Dysmorphol; 1993 Apr; 2(2):123-30. PubMed ID: 8281273
    [Abstract] [Full Text] [Related]

  • 2. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P.
    Genet Couns; 1993 Apr; 4(2):147-51. PubMed ID: 8395190
    [Abstract] [Full Text] [Related]

  • 3. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
    Thomas JA, Manchester DK, Prescott KE, Milner R, McGavran L, Cohen MM.
    Am J Med Genet; 1996 Apr 24; 62(4):372-5. PubMed ID: 8723067
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  • 4. Marfanoid features and craniosynostosis: report of one case and review.
    Lacombe D, Battin J.
    Clin Dysmorphol; 1993 Jul 24; 2(3):220-4. PubMed ID: 8287183
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  • 5. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.
    Lin HJ, Kakkis ED, Eteson DJ, Lachman RS.
    Am J Med Genet; 1993 Sep 15; 47(4):534-9. PubMed ID: 8256819
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  • 7. The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profile.
    De Smet L, Legius E, Fabry G, Fryns JP.
    Genet Couns; 1993 Sep 15; 4(2):157-64. PubMed ID: 8357567
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  • 8. Pfeiffer type cardiocranial syndrome: a third case report.
    Williamson-Kruse L, Biesecker LG.
    J Med Genet; 1995 Nov 15; 32(11):901-3. PubMed ID: 8592338
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  • 11. Feingold syndrome: report of a new family and review.
    Courtens W, Levi S, Verbelen F, Verloes A, Vamos E.
    Am J Med Genet; 1997 Nov 28; 73(1):55-60. PubMed ID: 9375923
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  • 12. Kaufman oculocerebrofacial syndrome in a girl of 15 years.
    Briscioli V, Manoukian S, Selicorni A, Livini E, Lalatta F.
    Am J Med Genet; 1995 Jul 31; 58(1):21-3. PubMed ID: 7573151
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  • 13. Anophthalmia-Waardenburg syndrome: a report of three cases.
    Suyugül Z, Seven M, Hacihanefioğlu S, Kartal A, Suyugül N, Cenani A.
    Am J Med Genet; 1996 Apr 24; 62(4):391-7. PubMed ID: 8723070
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  • 15. Twins and their mildly affected mother with Weaver syndrome.
    Dumić M, Vuković J, Cvitkovic M, Medica I.
    Clin Genet; 1993 Dec 24; 44(6):338-40. PubMed ID: 8131308
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  • 16. Craniosynostosis with Marfan syndrome, hand and foot anomalies.
    Shah AM, Chattopadhyay A, Kher A, Bharucha BA, Karapurkar AP.
    Clin Dysmorphol; 1996 Jul 24; 5(3):263-6. PubMed ID: 8818457
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  • 17. Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.
    Graham JM, Braddock SR, Mortier GR, Lachman R, Van Dop C, Jabs EW.
    Am J Med Genet; 1998 May 26; 77(4):322-9. PubMed ID: 9600744
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  • 18. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD, Dowton SB, McAlister WH, Waggoner DJ.
    Clin Genet; 2000 Jun 26; 57(6):444-8. PubMed ID: 10905665
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  • 19. Otospondylomegaepiphyseal dysplasia: report of three sibs and review of the literature.
    al Gazali LI, Lytle W.
    Clin Dysmorphol; 1994 Jan 26; 3(1):46-54. PubMed ID: 8205326
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  • 20. Holoprosencephaly and primary craniosynostosis: the Genoa syndrome.
    Camera G, Lituania M, Cohen MM.
    Am J Med Genet; 1993 Dec 01; 47(8):1161-5. PubMed ID: 8291548
    [Abstract] [Full Text] [Related]

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